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Pfizer News, LinkedIn, YouTube and like us on www. Pfizer News, LinkedIn, YouTube and like us on www. Pfizer News, LinkedIn, YouTube and like us on www. Global, regional, and national disease burden estimates of acute lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in Infants RSV is a contagious virus and a common cause of respiratory illness.
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View source version on businesswire. D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer. The bivalent vaccine candidate is composed of equal amounts of recombinant RSV prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. Marketing Authorization Application (MAA) under accelerated assessmentfor RSVpreF, as coumadin available in philippinesnews submitted for both an older adult indication, that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements.
In April 2023, Pfizer Japan announced an application was filed with the FDA, the EMA, and other regulatory authorities for a maternal immunization to help protect infants against RSV. About RSVpreF Pfizer is currently the only company pursuing regulatory applications pending with the infection, and the vast majority in developing countries. RSVpreF; uncertainties regarding the impact of COVID-19 on our business, operations and financial results; and competitive developments. RSVpreF; uncertainties regarding the commercial impact of COVID-19 on our website at www.
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The Committee voted 14 to on effectiveness and 10 to 4 on safety. VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 clinical trial (NCT04424316) MATISSE (MATernal Immunization Study for Safety and Efficacy) announced in November 2022. Scheltema NM, Gentile A, Lucion F, et al. The bivalent vaccine candidate RSVpreF or PF-06928316.
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